ENST00000360937.9:c.*81G>T
MANE Select
|
ENSP00000354193.4:n.*81G>T
|
|
ENST00000360937.8:c.*81G>T
|
ENSP00000354193.4:n.*81G>T
|
|
ENST00000467291.5:c.*81G>T
|
ENSP00000418328.1:n.*81G>T
|
|
ENST00000493429.5:c.*81G>T
|
ENSP00000418614.1:n.*81G>T
|
|
ENST00000622116.4:c.*329G>T
|
ENSP00000481520.1:n.*329G>T
|
|
NM_001091.3:c.*81G>T
|
NP_001082.2:n.*81G>T
|
|
NM_001272072.1:c.*81G>T
|
NP_001259001.1:n.*81G>T
|
|
XR_928169.1:n.295+15719C>A
|
|
|
XR_928170.1:n.425+7326C>A
|
|
|
XR_928171.1:n.297+15719C>A
|
|
|
XR_928169.2:n.301+15719C>A
|
|
|
XR_928171.2:n.301+15719C>A
|
|
|
NM_001091.4:c.*81G>T
MANE Select
|
NP_001082.2:n.*81G>T
|
|
NM_001272072.2:c.*81G>T
|
NP_001259001.1:n.*81G>T
|
|